Once-weekly GLP-1 agonists: How do they differ from exenatide and liraglutide?
Curr Diab Rep · 2010
Last updated 2026-05-28| Journal | Curr Diab Rep, 2010 |
|---|---|
| Citations | 34 |
| Relative citation ratio | 0.98 |
| NIH percentile | 50 |
| Molecules | liraglutide, exenatide |
| Conditions studied | Type 2 Diabetes, Obesity, Cardiovascular Risk Reduction |
Abstract
Incretin mimetics offer a new modality in diabetes treatment. This modality is based on the effects of the naturally occurring glucoregulatory gut hormone glucagon-like peptide-1 (GLP-1), which counteracts several pathophysiologic traits in type 2 diabetes. GLP-1 receptor agonists with extended half-lives entailing fewer injections and presumably an improved throughout-the-day glycemic control are in clinical development. This article summarizes the physiologic effects of GLP-1; the effects of the already marketed GLP-1 analogues for daily dosing, exenatide and liraglutide; and reviews the presently published data (with emphasis on clinical pharmacokinetics, efficacy, and safety) on GLP-1 agonists, which currently are in development and intended for once-weekly dosing: albiglutide/albugon, CJC-1131, CJC-1134-PC, exenatide once weekly, and taspoglutide.
Verbatim abstract via PubMed 20425571 ↗
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